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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522849Generated: October 26, 2026

Acetic Acid → N-(4-Bromobenzyl)-2,2-dimethoxyethanamine

https://huagongshe.com/reaction/522849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-BromobenzaldehydeHCID 70741—
ReactantAminoacetaldehyde dimethyl acetalHCID 89728—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductN-(4-Bromobenzyl)-2,2-dimethoxyethanamineHCID 5922624173%

Reaction Steps

To an ice-cold solution of 4-bromo-benzaldehyde (10 g, 0.05 mol) and 2,2-dimethoxy-ethylamine (6.8 g, 0.06 mol) in MeOH (200 mL) was added AcOH (2 mL), and the reaction mixture was stirred at RT for 1 h. The reaction mixture was cooled to 0° C. and NaBH4 (6.2 g, 0.15 mol) was added portionwise. The reaction mixture was stirred at RT for 10 h. After completion, The resulting reaction mixture was concentrated under reduced pressure and 10% aqueous NaOH was added. The mixture was extracted with EtOAc, the organic layer separated, dried over Na2SO4, and concentrated under reduced pressure. Purification was done by column chromatography using 100-200 mesh silica gel eluting with 5-15% EtOAc in hexanes to afford N-(4-bromobenzyl)-2,2-dimethoxyethanamine (10 g, 67%) as a pale yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334269B2
Source datasetuspto-grants-2016_05
ORD IDord-be8d3061f31b411a919d5233dcde361e
Source noteuspto-grants-2016_05